similar to: Covid Mutations: Cumulative?

In the context of the COVID-19 pandemic, Nasim Telecom decided to publish the first six-captures of Persian Asterisk book that was written by me and Mr Najafi, published in 2017. Also it was introduced by Mr. David Duffett in AstriCon 2017 on Florida. It would be useful for all people which understand Persian language, Also all other people could use it by going code commands on it and examples.

Hola a todos, Por fin pude terminar de preparar la descarga y procesamiento de los datos por edad y sexo. Ya están en el repositorio: https://github.com/rubenfcasal/COVID-19 Ya puestos también incluí la descarga e importación de los datos acumulados del ISCIII y actualicé las tablas en https://rubenfcasal.github.io/COVID-19/COVID-19-tablas.html empleando el paquete DT. Ahora tiene tres

Hi, As part of my dissertation, I'm going to be doing an Anova, comparing the "dead zone" diameters on plates of microbial growth with little paper disks "loaded" with antimicrobial, a clear zone appears where death occurs, the size depending on the strength and succeptibility. So it's basically 4 different treatments, and I'm comparing the diameters (in mm) of

Muchas gracias a todos por su ayuda. Hace un rato antes de abrir el correo, he encontrado dos soluciones a mi problema de como calcular el porcentaje de variación. La primera es usando el paquete dplyr: https://stackoverflow.com/questions/48196552/calculate-percentage-change-in-r-using-dplyr/48196871 La segunda usando la función PercChange del paquete DataCombine

On 25/02/2011 21:22, Ben Ward wrote: > > -------- Original Message -------- > Subject: Re: [R] ANOVA and Pseudoreplication in R > Date: Fri, 25 Feb 2011 12:10:14 -0800 > From: Bert Gunter<gunter.berton at gene.com> > To: Ben Ward<benjamin.ward at bathspa.org> > CC: r-help<r-help at r-project.org> > > > > I can hopefully save bandwidth here by

Eric ¿Que dataset utilizo? Por curiosidad probé su código, pero me salen errores. Copio y pego todo como me sale en la consola. > # https://raw.githubusercontent.com/datasets/covid-19/master/data/time-series-19-covid-combined.csv > datos <- read.csv("C:/Users/HP/Downloads/time-series-19-covid-combined.csv") > > library(data.table) > library(ggplot2) >

Hola: Tengo los datos diarios del número de casos de coronavirus por comunidades autónomas y quiero calcular el número diario de nuevos casos y la tasa diaria de variación del número de casos y no se como hacerlo en R. *fecha* *comunidad* *poblacion* *casos_totales* 04/03/2020 Andalucía 8414240 13 05/03/2020 Andalucía 8414240 12 06/03/2020 Andalucía 8414240 21 04/03/2020 Aragón

Gracias Ruben, muy interesante. Algo así estuve buscando, por ciudades y a nivel internacional, pero no lo encontré. Me bastaría con el número de fallecimientos por día, de cuantas más ciudades del mundo mejor. Si alguno supiera de algo así, le agradecería que me lo comunicase. Un saludo, Manuel El mar., 24 mar. 2020 a las 21:04, Rubén Fernández Casal (< rubenfcasal en gmail.com>) escribió:

Hi all, This is really a stats question as much as an R question. I'm trying to do a joint scaling test (JST - see below) on some very oddly-distributed data and was wondering if anyone can suggest a good way of dealing with model violations and/or using R to evaluate how sensitive the model is to violations of the normality assumption. Here's a quick explanation of the analysis, the

On Fri, 2005-06-03 at 09:36, Simon Perreault wrote: > i'm not sure you've considered your position thoroughly. > I am, and I will say it again just for the shock value: > Red Hat is the main developer of CentOS. On Fri, 3 Jun 2005, Les Mikesell wrote: > I'd put it this way instead: Red Hat is responsible for any > difficulty in creating the CentOS distribution, while

Hi, I'm doing some modelling (lm) for my 3rd year dissertation and I want to do some resampling, especially as I'm working with microbes, getting them to evolve resistance to antimicrobial compounds, and after each exposure I'm measuring the minimum concentration required to kill them (which I'm expecting to rise over time, or exposures), I have 5 lineages per cleaner, and

Hi, I've been doing an experiment, measuring the dead-zone-diameters of bacteria, when they've been grown with paper diffusion disks of antimicrobial. There are two groups, or treatments - one is bacteria that have been cultured in said antimicrobial for the past year, the other group is of the same species, but lab stock and has not gone had any prior contact with the antimicrobial.

On Apr 20, 2012, at 10:31 AM, dag at cray.com wrote: > I'd like to begin a project to rework the scheduler to address some > problems we've discovered on this end. The goal is to get a more > configurable/flexible scheduler while simplifying maintenance by > separating policy from implementation to get independent and > interchangeable parts. > > This is going to be

Dear all, I wanted to let you know about four phylogenetic comparative methods (PCM) packages that have become available on (3 on CRAN and 1 on GitHub) recently that hopefully will be interesting to somebody. Three of them go significantly beyond the Brownian motion (BM) and Ornstein-Uhlenbeck (OU) processes. 1) There is a new version of mvSLOUCH available. The most important change is that the

Dear all, I wanted to let you know about four phylogenetic comparative methods (PCM) packages that have become available on (3 on CRAN and 1 on GitHub) recently that hopefully will be interesting to somebody. Three of them go significantly beyond the Brownian motion (BM) and Ornstein-Uhlenbeck (OU) processes. 1) There is a new version of mvSLOUCH available. The most important change is that the

Hi, I've been modelling some data over the past few days, of my work, repeatedly challenging microbes to a certain concentration of cleaner, until the required concentration to inhibit or kill them increaces, at which point they are challenged to a slightly higher concentration each day. I'm doing ths for two different cleaners and I'm collecting the required concentration to

Hi everyone I am sending mails with rails in German. The Problem is that the German letters ä,ü,ö are arriving correctly at the receiver. When the subject contains the word Für the receiver gets Für Does anybody knows this issue? Thanks in advance. Adam -- Posted via http://www.ruby-forum.com/.

-------- Original Message -------- Subject: Re: [R] Simulation - Natrual Selection Date: Wed, 05 Jan 2011 17:24:05 +0000 From: Ben Ward <benjamin.ward@bathspa.org> To: Bert Gunter <gunter.berton@gene.com> CC: Mike Marchywka <marchywka@hotmail.com> On 05/01/2011 17:08, Bert Gunter wrote: > Couple of brief comments inline below. -- Bert > > On Wed, Jan 5, 2011 at

Andrew Trick <atrick at apple.com> writes: > We plan to move to the MachineScheduler by 3.2. The structure is: How hard will this be to backport to 3.1? Has woprk on this started yet? > ScheduleDAG: Abstract DAG of SUnits and SDeps > | > v > ScheduleDAGInstrs: Build the DAG from MachineInstrs, each SUnit tied to an MI > Delimit the current

Hey Everyone, I'd like to begin a project to rework the scheduler to address some problems we've discovered on this end. The goal is to get a more configurable/flexible scheduler while simplifying maintenance by separating policy from implementation to get independent and interchangeable parts. This is going to be challenging because we are still stuck on LLVM 2.9. We will be upgrading